Canonical Allele Identifier: CA1385038398
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93896813_93896817delinsATAAT , CM000665.2:g.93896813_93896817delinsATAAT GRCh38
NC_000003.11:g.93615657_93615661delinsATAAT , CM000665.1:g.93615657_93615661delinsATAAT GRCh37
NC_000003.10:g.95098347_95098351delinsATAAT NCBI36
NG_009813.1:g.82274_82278delinsATTAT , LRG_572:g.82274_82278delinsATTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.850-126_850-122delinsATTAT ENSP00000330021.7:n.850-126_850-122delinsATTAT
ENST00000394236.9:c.850-126_850-122delinsATTAT MANE Select ENSP00000377783.3:n.850-126_850-122delinsATTAT
ENST00000407433.6:c.805-126_805-122delinsATTAT ENSP00000385794.2:n.805-126_805-122delinsATTAT
ENST00000647936.1:c.850-126_850-122delinsATTAT ENSP00000496822.1:n.850-126_850-122delinsATTAT
ENST00000648381.1:n.1018-126_1018-122delinsATTAT
ENST00000648853.1:c.808-126_808-122delinsATTAT ENSP00000497262.1:n.808-126_808-122delinsATTAT
ENST00000649103.1:c.949-126_949-122delinsATTAT ENSP00000497962.1:n.949-126_949-122delinsATTAT
ENST00000650591.1:c.946-126_946-122delinsATTAT ENSP00000497376.1:n.946-126_946-122delinsATTAT
ENST00000394236.7:c.850-126_850-122delinsATTAT ENSP00000377783.3:n.850-126_850-122delinsATTAT
ENST00000407433.5:c.457-126_457-122delinsATTAT ENSP00000385794.1:n.457-126_457-122delinsATTAT
NM_000313.3:c.850-126_850-122delinsATTAT , LRG_572t1:c.850-126_850-122delinsATTAT NP_000304.2:n.850-126_850-122delinsATTAT
NM_001314077.1:c.946-126_946-122delinsATTAT , LRG_572t2:c.946-126_946-122delinsATTAT NP_001301006.1:n.946-126_946-122delinsATTAT
NM_000313.4:c.850-126_850-122delinsATTAT MANE Select NP_000304.2:n.850-126_850-122delinsATTAT
NM_001314077.2:c.946-126_946-122delinsATTAT NP_001301006.1:n.946-126_946-122delinsATTAT